Variants in gene CACNA1S with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_000069.3(CACNA1S):c.900G>A (p.Trp300Ter)	rs148317787	0.00004
NM_000069.3(CACNA1S):c.1234C>T (p.Arg412Ter)	rs767052156	0.00001
NM_000069.3(CACNA1S):c.2269C>T (p.Arg757Ter)	rs770073633	0.00001
NM_000069.3(CACNA1S):c.2707C>T (p.Arg903Ter)	rs367983954	0.00001
NM_000069.3(CACNA1S):c.502C>T (p.Arg168Ter)	rs201998231	0.00001
NM_000069.3(CACNA1S):c.520C>T (p.Arg174Trp)	rs772226819	0.00001
NM_000069.3(CACNA1S):c.1401_1414del (p.Asn468fs)	rs2102144416
NM_000069.3(CACNA1S):c.1847G>A (p.Trp616Ter)	rs1572048220
NM_000069.3(CACNA1S):c.2627T>A (p.Val876Glu)	rs267606698
NM_000069.3(CACNA1S):c.2690G>C (p.Arg897Thr)	rs1287079817
NM_000069.3(CACNA1S):c.2812del (p.Leu938fs)	rs1572038993

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